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Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- AUERBACH V. H., DIGEORGE A. M., BRIGHAM M. P., DOBBS J. M. Delayed maturation of tyrosine metabolism in a full-term sibling of a child with phenylketonuria. J Pediatr. 1963 Jun;62:938–940. doi: 10.1016/s0022-3476(63)80113-4. [DOI] [PubMed] [Google Scholar]
- Avery M. E., Clow C. L., Menkes J. H., Ramos A., Scriver C. R., Stern L., Wasserman B. P. Transient tyrosinemia of the newborn: dietary and clinical aspects. Pediatrics. 1967 Mar;39(3):378–384. [PubMed] [Google Scholar]
- KLEINMAN D. S. PHENYLKETONURIA. A REVIEW OF SOME DEFICITS IN OUR INFORMATION. Pediatrics. 1964 Jan;33:123–134. [PubMed] [Google Scholar]
- PARTINGTON M. W., ANDERSON R. M. CASE-FINDING IN PHENYLKETONURIA. I. REPORT OF A SURVEY BY THE COLLEGE OF GENERAL PRACTICE OF CANADA. Can Med Assoc J. 1964 Jun 6;90:1312–1314. [PMC free article] [PubMed] [Google Scholar]
- Partington M. W. Case-finding in phenylketonuria: 3. One-way paper chromatography of amino acids in blood. Can Med Assoc J. 1968 Oct 5;99(13):638–644. [PMC free article] [PubMed] [Google Scholar]
- Schneider A. J., Garrard S. D. Diagnostic and therapeutic implications of persistent hyperphenylalaninemia in an infant heterozygous for the gene of phenylketonuria. J Pediatr. 1966 May;68(5):704–712. doi: 10.1016/s0022-3476(66)80442-0. [DOI] [PubMed] [Google Scholar]